Pharmaceutical dispersion techniques for dissolution and bioavailability enhancement of poorly water-soluble drugs
X Zhang, H Xing, Y Zhao, Z Ma - Pharmaceutics, 2018 - mdpi.com
Over the past decades, a large number of drugs as well as drug candidates with poor
dissolution characteristics have been witnessed, which invokes great interest in enabling …
dissolution characteristics have been witnessed, which invokes great interest in enabling …
[HTML][HTML] Liquisolid technique and its applications in pharmaceutics
M Lu, H Xing, J Jiang, X Chen, T Yang, D Wang… - Asian journal of …, 2017 - Elsevier
Most of the newly developed drug candidates are lipophilic and poorly water-soluble.
Enhancing the dissolution and bioavailability of these drugs is a major challenge for the …
Enhancing the dissolution and bioavailability of these drugs is a major challenge for the …
Formation of nanosuspensions in bottom-up approach: theories and optimization
A Ahmadi Tehrani, MM Omranpoor, A Vatanara… - DARU Journal of …, 2019 - Springer
Background Nanosuspensions, liquid dispersions with nanometer size distribution, are
becoming trendy in pharmaceutical practice to formulate poorly water-soluble drugs and to …
becoming trendy in pharmaceutical practice to formulate poorly water-soluble drugs and to …
Lipid nanocapsules enhance the transdermal delivery of drugs regardless of their physico-chemical properties
A Kalvodová, J Zbytovská - International Journal of Pharmaceutics, 2022 - Elsevier
The transdermal application of actives offers numerous advantages over other conventional
routes. Namely, a stable level of drugs in the bloodstream and reduced side effects are the …
routes. Namely, a stable level of drugs in the bloodstream and reduced side effects are the …
Liquisolid systems and aspects influencing their research and development
B Vraníková, J Gajdziok - Acta pharmaceutica, 2013 - hrcak.srce.hr
Sažetak Many modern drugs are poorly water soluble substances, which causes difficulties
in the development of solid dosage forms with sufficient bioavailability. Preparation of …
in the development of solid dosage forms with sufficient bioavailability. Preparation of …
Comparative study of powder carriers physical and structural properties
K Kostelanská, BB Prudilová, S Holešová, J Vlček… - Pharmaceutics, 2022 - mdpi.com
High specific surface area (SSA), porous structure, and suitable technological characteristics
(flow, compressibility) predetermine powder carriers to be used in pharmaceutical …
(flow, compressibility) predetermine powder carriers to be used in pharmaceutical …
The first zwitterionic cocrystal of indomethacin with amino acid showing optimized physicochemical properties as well as accelerated absorption and slowed …
LY Wang, YM Yu, FB Jiang, YT Li, ZY Wu… - New Journal of …, 2020 - pubs.rsc.org
The first zwitterionic cocrystal of indomethacin (INC) with amino acid, INC–PL-H2O, where
PL represents L-proline, was prepared and thoroughly characterized by single crystal and …
PL represents L-proline, was prepared and thoroughly characterized by single crystal and …
Dissolution enhancement of tadalafil by liquisolid technique
M Lu, H Xing, T Yang, J Yu, Z Yang… - Pharmaceutical …, 2017 - Taylor & Francis
This study aimed to enhance the dissolution of tadalafil, a poorly water-soluble drug by
applying liquisolid technique. The effects of two critical formulation variables, namely drug …
applying liquisolid technique. The effects of two critical formulation variables, namely drug …
[HTML][HTML] The most recent advances in liquisolid technology: Perspectives in the pharmaceutical industry
Hydrophobic drugs exhibit altered bioavailability and pose other challenges at an industrial
level due to their poor solubility and dissolution rates. In addition, poor flowability …
level due to their poor solubility and dissolution rates. In addition, poor flowability …
Modern evaluation of liquisolid systems with varying amounts of liquid phase prepared using two different methods
B Vraníková, J Gajdziok… - BioMed research …, 2015 - Wiley Online Library
Liquisolid systems are an innovative dosage form used for enhancing dissolution rate and
improving in vivo bioavailability of poorly soluble drugs. These formulations require specific …
improving in vivo bioavailability of poorly soluble drugs. These formulations require specific …